[Recalled] TAUT, Cholangiogram Catheter Intraducer, Peritoneal Catheter, Teleflex Medical, Research Triangle Park, NC. An introduction/drainage catheter accessory is intended to aid in the manipulation of or insertion of the device into
This is an official product-safety recall record. Below are the verified details from the issuing authority, in plain language.
Recall details
| Product | TAUT, Cholangiogram Catheter Intraducer, Peritoneal Catheter, Teleflex Medical, Research Triangle Park, NC. An introduction/drainage catheter accessory is intended to aid in the manipulation of or insertion of the device into the body. |
|---|---|
| Brand / manufacturer | Teleflex Medical |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2186-2012 |
| Country of notice | United States |
| Risk level | Class III |
| Hazard type | recall |
| Notice date | 20 July 2012 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: Product is missing the label on the internal packaging.
This Class III recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Teleflex Medical
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.
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